Canonical Allele Identifier: PA2827999670
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln2745His
CA10582345
NM_001354901.2:c.8235G>T
CA16039584
NM_001354901.2:c.8235G>C